K. Kekou: search on Z-Library

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1

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

Bladen, Catherine L., Salgado, David, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Roy, Anna J., Chamova, Teodora, Guergueltcheva, Velina,

Journal:

Year:

2015

Language:

english

File:

PDF, 646 KB

english, 2015

2

Phenotypic variability and molecular genetics in proximal myotonic myopathy

Papadimas, George Konstantinos, Kekou, Kiriaki, Papadopoulos, Constantinos, Kararizou, Evangelia, Kanavakis, Emmanuel, Manta, Panagiota

Journal:

Year:

2015

Language:

english

File:

PDF, 2.22 MB

english, 2015

3

Identification of three polymorphisms in the dystrophin gene

K Kekou, A Mavrou, C Sofocleous, C Metaxotou

Journal:

Molecular and Cellular Probes

Year:

1999

Language:

english

File:

PDF, 89 KB

english, 1999

4

A simplified approach for FSHD molecular testing

Papanikos, Frantzeskos, Skoulatou, Christina, Sakellariou, Paraskevi, Kekou, Kyriaki, Christopoulos, Theodore K., Kanavakis, Emmanuel, Traeger-Synodinos, Jan, Ioannou, Penelope C.

Journal:

Clinica Chimica Acta

Year:

2014

Language:

english

File:

PDF, 926 KB

english, 2014

5

Mutation spectrum and phenotypic manifestation in FSHD Greek patients

P. Sakellariou, K. Kekou, H. Fryssira, C. Sofocleous, P. Manta, A. Panousopoulou, K. Gounaris, E. Kanavakis

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 691 KB

english, 2012

6

Tall Stature, Insulin Resistance, and Disturbed Behavior in a Girl with the Triple X Syndrome Harboring Three SHOX Genes: Offspring of a Father with Mosaic Klinefelter Syndrome but with Two Maternal X Chromosomes

Kanaka-Gantenbein, Christina, Kitsiou, Sophia, Mavrou, Ariadni, Stamoyannou, Lela, Kolialexi, Aggeliki, Kekou, Kyriaki, Liakopoulou, Magda, Chrousos, George

Journal:

Hormone Research

Year:

2004

Language:

english

File:

PDF, 121 KB

english, 2004

7

Early onset cataract: prominent feature in myotonic dystrophy type 2

Papadopoulos, C., Xirou, S., Kekou, K., Kitsiou-Tzeli, S., Kararizou, E., Papadimas, G.

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 247 KB

english, 2017

8

P295 – 1801 A single aminoacid deletion in the dystrophin protein associated with a mild clinical phenotype

Pons, R, Kekou, K, Gkika, A, Vogiatzakis, N, Svigou, M, Papadimas, G, Youroukos, S, Kanavakis, M

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 63 KB

english, 2013

9

Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol

Nikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, Sophia Kitsiou, Ariadni Mavrou, Chrisa Bakoula, Emmanouel Kanavakis

Journal:

Molecular Biotechnology

Year:

2007

Language:

english

File:

PDF, 370 KB

english, 2007

10

Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome

S. Voutoufianakis, S. Psoni, P. Vorgia, F. Tsekoura, K. Kekou, J. Traeger-Synodinos, S. Kitsiou, E. Kanavakis, H. Fryssira

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 518 KB

english, 2007

11

P03.3 Clinical, biochemical and molecular analysis of patients with chronic subclinical elevation of CK and recurrent hyperCKemia

R. Pons, A. Gika, K. Kekou, N. Vogiatzakis, G. Nikas, E. Kanavakis, P. Manta, A. Ribes, A. Andreu, E. Garcia-Arumi, E. Michelakaki, S. Youroukos

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 52 KB

english, 2011

12

Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol

Nikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous…

Journal:

Molecular Biotechnology

Year:

2013

Language:

english

File:

PDF, 467 KB

english, 2013

13

Cities in digital format

Journal:

Technoetic Arts a Journal of Speculative Research

Year:

2013

Language:

english

File:

PDF, 784 KB

english, 2013

14

Coinheritance of Noonan syndrome and Becker muscular dystrophy

Argirios Dinopoulos, Anna Papadopoulou, Panagiota Manta, Kiki Kekou, Tassos Kanelopoulos, Andreas Fretzayas, Sofia Kitsiou

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 127 KB

english, 2010

15

Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's disease

Pons, Roser, Kekou, Kyriaki, Antonellou, Roubina, Svingou, Maria, Kanavakis, Emmanouel, Stefanis, Leonidas

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 111 KB

english, 2016

16

A dynamic trinucleotide repeat (TNR) expansion in the DMD GENE

Kekou, Kyriaki, Sofocleous, Christalena, Papadimas, George, Petihakis, Dimitris, Svingou, Maria, Pons, Roser-Maria, Vorgia, Pelagia, Gika, Artemis, Kitsiou, Sophia, Kanavakis, Emmanuel

Journal:

Molecular and Cellular Probes

Year:

2016

Language:

english

File:

PDF, 2.02 MB

english, 2016

17

3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype

Kiriaki Kekou, Dr. Lina Florentin, Catherine Metaxotou

Journal:

Year:

1998

Language:

english

File:

PDF, 747 KB

english, 1998

18

Differential expression of tenascin-C in the developing human lung: an immunohistochemical study

M. Lambropoulou, V. Limberis, N. Koutlaki, M. Simopoulou, D. Ntanovasilis, G. P. Vandoros, P. Tatsidou, I. Kekou, I. Koutsikogianni, N. Papadopoulos

Journal:

Clinical and Experimental Medicine

Year:

2009

Language:

english

File:

PDF, 430 KB

english, 2009

19

043 Spinal muscular atrophy in Greece

S. Youroukos, K. Kekou, G. Konstantinidis, C. Bili, L. Florentin, H. Frysira, C. Tsengi, C. Metaxotou

Journal:

European Journal of Paediatric Neurology

Year:

1999

Language:

english

File:

PDF, 282 KB

english, 1999

20

A single amino acid loss in the dystrophin protein associated with a mild clinical phenotype

Pons, Roser, Kekou, Kyriaki, Gkika, Artemis, Papadimas, George, PhD, NikolaosVogiatzakis, Svingou, Maria, Papadopooulos, Constantinos, Nikas, Ioanis, Dinopoulos, Argirios, Youroukos, Sotiris, Kanavaki

Journal:

Year:

2016

Language:

english

File:

PDF, 650 KB

english, 2016

21

Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database

Koeks, Zaïda, Bladen, Catherine L., Salgado, David, van Zwet, Erik, Pogoryelova, Oksana, McMacken, Grace, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamo

Journal:

Journal of Neuromuscular Diseases

Year:

2017

Language:

english

File:

PDF, 444 KB

english, 2017

22

Caveolinopathies in Greece

Papadopoulos, Constantinos, Papadimas, George K., Kekou, Kyriaki, Spengos, Konstantinos, Svigou, Maria, Kitsiou-Tzeli, Sofia, Manta, Panagiota

Journal:

The Neurologist

Year:

2015

Language:

english

File:

PDF, 211 KB

english, 2015

23

SURVEYOR on the Spot

Vogiatzakis, Nikolaos, Kekou, Kyriaki, Sophocleous, Christalena, Kitsiou, Sophia, Mavrou, Ariadni, Bakoula, Chrisa, Kanavakis, Emmanouel, Deltas, Constantinos, Voskarides, Konstantinos

Journal:

The Journal of Molecular Diagnostics

Year:

2010

Language:

english

File:

PDF, 46 KB

english, 2010

24

Early onset posterior subscapular cataract in a series of myotonic dystrophy type 2 patients

Papadopoulos, C, Kekou, K, Xirou, S, Kitsiou-Tzeli, S, Kararizou, E, Papadimas, G K

Journal:

Year:

2017

Language:

english

File:

PDF, 88 KB

english, 2017

25

Association of VEGF Gene Polymorphisms with the Development of Heart Failure in Patients after Myocardial Infarction

Douvaras, Panagiotis, Antonatos, Dionisios G., Kekou, Kiriaki, Patsilinakos, Sotirios, Chouliaras, George, Christou, Apostolos, Andrikou, Anastasios, Kanavakis, Emmanuel

Journal:

Year:

2009

Language:

english

File:

PDF, 153 KB

english, 2009

26

Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients

Skouteli, Helen N, Metaxotou, Catherine, Kekou, Kiriaki, Mavrou, Ariadni, Florentin, Lina, Youroukos, Sotiris, Zafiriou, Dimitrios I

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 310 KB

english, 1999

27

Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years

Kekou, Kyriaki, Svingou, Maria, Sofocleous, Christalena, Mourtzi, Niki, Nitsa, Evangelia, Konstantinidis, George, Youroukos, Sotiris, Skiadas, Konstantinos, Katsalouli, Marina, Pons, Roser, Papavasile

Journal:

Journal of Neuromuscular Diseases

Year:

2020

File:

PDF, 366 KB

2020

28

Mapping dystrophin gene recombinants in Greek DMD/BMD families: low recombination frequencies in the STR region

Lina Florentin, Chrysanthy Bili, Kiriaki Kekou, Nicolaos Tripodis, Ariadni Mavrou, Catherine Metaxotou

Journal:

Year:

1995

Language:

english

File:

PDF, 508 KB

english, 1995

29

Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol

Kiriaki Kekou, Helena Fryssira, Christalena Sophocleous, Ariadni Mavrou, Panagiota Manta, Catherine Metaxotou

Journal:

Molecular and Cellular Probes

Year:

2005

Language:

english

File:

PDF, 112 KB

english, 2005

30

PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol

C Christofidou, C Sofocleous, C Vrettou, A Destouni, J Traeger-Synodinos, K Kekou, G Palmer, G Kokkali, A Mavrou, S Kitsiou, E Kanavakis

Journal:

Reproductive BioMedicine Online

Year:

2009

Language:

english

File:

PDF, 489 KB

english, 2009

31

SMA prenatal diagnosis: A modified protocol to help differentiation between deletions and gene conversion

Kekou, K., Sofocleous, C., Konstantinidis, G., Fryssira, H., Mavrou, A., Kitsiou, S., Kanavakis, E.

Journal:

Molecular and Cellular Probes

Year:

2015

Language:

english

File:

PDF, 275 KB

english, 2015

32

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

Florentin, L, Mavrou, A, Kekou, K, Metaxotou, C

Journal:

Journal of Medical Genetics

Year:

1995

Language:

english

File:

PDF, 597 KB

english, 1995

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